![]() Method of producing hydrocarbon distillate fractions
专利摘要:
Distillates are produced from asphaltenes-containing hydrocarbon mixtures by a process comprising subjecting the hydrocarbon mixtures to thermal cracking, and subjecting the resulting heavy fraction to a combination of a catalytic hydrotreatment and a solvent deasphalting. 公开号:SU1424740A3 申请号:SU833568910 申请日:1983-03-16 公开日:1988-09-15 发明作者:Бартелд Квант Питер;Роберт Ньюсом Джон 申请人:Шелл Интернэшнл Рисерч Маатсхаппий Б.В. (Фирма); IPC主号:
专利说明:
4: GO four: CM The invention relates to a process for the production of distillate hydrocarbon fractions from asphaltene-containing hydrocarbon oil. The purpose of the invention is to increase the yield of target products. Embodiments of the invention are further sub-divided according to whether the heavy fraction from the thermal cracking treatment product is used as a starting material, or a component of the starting material for catalytic hydroprocessing (NT) (class IIIA), or as a starting material, or a component of a starting material for treatment of dissolving deasphalting (YES) (class IIIB). In the variant belonging to class IIIA, the heavy fraction extracted from the product of catalytic hydrotreatment (NT) is used as a starting material for processing solvent deasphalting (YES). In the embodiments belonging to class II1B, the asphalt bitumen fraction is used as catalytic hydrotreating (NT) feedstock, and the heavy fraction from the catalytic hydrotreating (NT) product is used as a component of the starting material for heat treatment king, or as a component of the starting material for treatment of dissolving deasphalting (DA), individually or in combination with these treatments. In the proposed process, the raw material used is a hydrocarbon mixture containing asphaltenes. A suitable parameter for estimating the content of asphaltenes in a hydrocarbon mixture, as well as reducing the content of asphaltenes, which appears when the hydrocarbon mixture containing asphaltenes is subjected to catalytic hydrotreatment (NT), is the RCT test value. A higher content of asphaltenes in the hydrocarbon mixture gives a higher value of the Ramsbottom (RCT) coke sample. Preferably, this process is applied to hydrocarbon mixtures that boil at temperatures substantially higher than 350 ° C and 35 °. 0 five 0 five 0 five 0 five 100 wt.% Of which boils at Bbraie temperatures of 520 ° C and which have a value of a Cox sample according to Remsbottom 7.5-50 wt. Examples of such hydrocarbon mixtures are residues obtained during the distillation of various types of crude oil, as well as heavy hydrocarbon mixtures derived from oil shale and butuminous sand. If required, this process can also be applied to heavy crude mineral oils, residues from thermal cracking of hydrocarbon mixtures, and asphalt bitumen obtained from solvent-based asphaltenes from hydrocarbon mixtures. Hydrocracking is carried out at 300 -, in particular at 350-450 s, pressure 50-300 bar, in particular 75-200 bar, volume equilibrium rate 0.02-10 g X g X, in particular 0.1-2 g XX, and with the ratio H, the base material is 100-5000 Nl x X kg, in particular 500-2000 Nl x X KG. The second or third step is deasphalting, in which the raw material containing asphaltenes is converted into a product from which the deasphalted oil is separated into a fraction and an asphalt bituminous fraction. Suitable solvents for deasphalting are paraffin hydrocarbons having 3 to 6 carbon atoms per molecule, such as p-butane, and mixtures thereof, such as mixtures of propane and p-butane, and mixtures of p-butane and p-pentane. Suitable weight ratios of solvent: the oil lies within (7: 1) - (1: 1), in particular between 4: 1 and 1: 1. The deasphalting (YES) treatment is carried out at a pressure of 20-100 bar. When p-butane is used as a solvent, deasphalting is carried out at a pressure of 35-45 bar and at a temperature of 100-150 C. Three technological schemes for the production of distillates of petroleum oils from asphaltenes containing hydrocarbon mixtures according to the proposed method are explained in more detail below. Technological scheme A. The process is carried out in a system containing successively a thermal cracking zone composed of a thermal cracking unit, a distillation unit at atmospheric pressure, a second thermal cracking unit, a second distillation unit at atmospheric pressure and a vacuum distillation unit, a catalytic hydrotreating zone composed of catalytic hydroprocessing, a third distillation unit at atmospheric pressure, and a second vacuum distillation unit and a dissolving deasphaltine zone Vani. The asphaltenes-containing hydrocarbon mixture is mixed with a stream of asphalt bitumen and this mixture is subjected to thermal cracking. The resulting thermal cracked product is separated by distillation at atmospheric pressure into a gas fraction obtained by distillation at atmospheric pressure distillate and residue. The residue obtained by distillation at atmospheric pressure is mixed with the residue obtained by distillation at atmospheric pressure and this mixture is separated by vacuum distillation into a vacuum distillate and a vacuum residue. The vacuum residue is subjected to catalytic hydroprocessing along with hydrogen. The hydrotreated product is separated by distillation at atmospheric pressure into a gas fraction obtained by distillation at atmospheric pressure, the distillate and the residue. The residue obtained by distillation at atmospheric pressure is separated by vacuum distillation into a vacuum distiller and a vacuum residue. The vacuum residue is separated by dissolving deasphalting into deasphalted oil and asphalt bitumen. De-asphalt oil is subjected to thermal cracking. The thermally cracked product is separated by distillation at atmospheric pressure into a gas fraction obtained by distillation at atmospheric pressure and a residue obtained by distillation at atmospheric pressure. Gas fractions are combined to form the mixture. Asphalt bitumen is divided into two hours. ti. I Technological Scheme B. The process is carried out in the same system and in the same way as described in techno 5 s 0 g - five logic diagram A, but the asphalt bitumen stream is mixed with the stream instead of the stream. Technological scheme C. The process is carried out in the system, successively containing a thermal cracking zone composed of a thermal cracking unit, a distillation unit at atmospheric pressure, a second thermal cracking unit, a second distillation unit at atmospheric pressure and a vacuum distillation unit, solvent deasphalting eon and zone catalytic hydroprocessing, composed of a catalytic hydroprocessing unit, a third distillation unit at atmospheric pressure and a second vacuum distillation unit Novki. The asphaltenes-containing hydrocarbon mixture is subjected to thermal cracking and the product obtained by thermal cracking is separated by distillation at atmospheric pressure into a gas fraction obtained by distillation at atmospheric pressure and the residue obtained by distillation at atmospheric pressure. The resultant distillation at atmospheric pressure is mixed with the resultant distillation at atmospheric pressure, and this mixture is separated by vacuum distillation into a vacuum distillate and a vacuum residue. The vacuum residue is mixed with the vacuum residue and this mixture is separated by dissolving deasphalting into deasphalted oil and asphalt bitumen. Asphalt bitumen is divided into two parts. The part is subjected, together with hydrogen, to catalytic hydroprocessing. The product obtained by hydrotreating is separated by distillation at atmospheric pressure into a gas fraction obtained by distillation at atmospheric pressure and distilled to a residue obtained by distillation at atmospheric pressure. The atmospheric residue is separated by vacuum distillation into a vacuum distillate and a vacuum residue. Deasphalted oil is subjected to thermal cracking. The resulting thermal cracked product is separated by distillation at atmospheric pressure into the gas fraction obtained by distillation at atmospheric pressure is distilled and the residue obtained by distillation at atmospheric pressure. Gas fractions are pooled. The distillates obtained by distillation at atmospheric pressure are combined. Example 1. Carried out according to the technological scheme A. 100 p.p. vacuum residue, ime tse value coke The initial mixtures used by Remsbottom 20.2 wt.% Yield In the proposed process, there are two asphaltene-containing hydrocarbon mixtures obtained as residues from vacuum distillation from distillation residues at atmospheric pressure from SF mineral oils. Both vacuum residues are boiled at a temperature of 520 ° C. They are Rothbottpm coke (RCT) values. ) 20.2 and 10.1 wt.%, Respectively. The process is carried out according to the technological schemes A - C. The following conditions are used in different zones. In all technological schemes, the installation for catalytic hydrotreatment contains two reactors, the first of which is filled with Ni / V / SiO — a catalyst containing 0.5 parts per volt (rf) nickel and 2.0 hours. pv vanadium at 100 ppt. silicon dioxide, and the second reactor, which is filled with a Co / Mo / AljOj catalyst containing 4 p.p. alumina, these catalysts are used in a 1: 4 volume ratio. The catalytic hydroprocessing is carried out at a hydrogen pressure of 150 bar, the weight feed rate per unit of catalyst weight (measured for both reactors) kg of starting material per liter of catalyst per hour, the ratio of N / starting material is about 1000 Nl per kg and the average temperature is 410 ° C in the first reactor and 385 C in the second reactor. In all technological schemes, the treatment of dissolving deasphalting is carried out using n-butane as a solvent, at 115 ° C, a pressure of 40 bar and a weight ratio of solvent: oil 3: 1, In all technological schemes, thermal cracking is carried out in two cracking coils, at a pressure of 20 bar, a volume-weight rate of 0.4 kg of fresh raw material per liter of cracking coil volume per minute, and temperature 480 С 4954 in the first cracking coil and in the second cracking coil (temperatures were measured at the outputs of the cracked coils). Example 1. Carried out according to the technological scheme A. 100 p.p. vacuum residue, ime tse value coke 50 five different streams of liquids c.p.: Ct-C gaseous fraction Mixture of flows, which was important for a sample of coke according to Remsbottom 23.5 wt.% 350 ° C atmospheric residue Mixture (321) The following vacuums are five 0 five 0 350-520 Ny distillate 520 ° С vacuum residue having a value of a sample for coke according to Remsbottom 30.8 wt.% of product (324), С, fraction of which had a value of test for coke according to Remsbottom 15.4 wt.% Su - 350 ° C atmospheric distillate 350 atmospheric residue 350-520 С vacuum distillate 520 ° С vacuum residue Deasphalted oil Asphalt bitumen Cj. - 350 ° C atmospheric distillate atmospheric residue Part Part 8.4 118.0 93.6 102.8 19.5 83.3 12.7 68.8 22.2 46.6 18.6 28.0 25.4 9.2 18.0 10.0 Example 2, embodied according to the technological scheme B. 100 h, p. vacuum residue having a coke sample value to 20 wt.%, give an output of various flows in the following quantities, ch.p.v .: Gaseous fraction 3.32 350 ° C atmospheric residue 82.2 Mixture98.9 350-5204 vacuum distillate 18.4 520 ° С vacuum residue 80.5 The mixture of streams, which is the value of the sample for coke according to Remsbottom, is 31.2 wt.% Of the product. Su, the fraction of which is important for a coke test according to Remsbottom 15.6 masl 101.0 С, is 350 ° С atmospheric distillate 16.8 atmospheric residue 78.2 350-520 s vacuum distillate 25.5 520 ° С vacuum o statok52,7 Deasphalted oil26,9 Asphalt bitumen 25.8; C5 - C50 with atmospheric distillate t 24.7 350 C atmospheric residue Part Part Example 3. In-process flow with 100 h, p. Vacuum-relevant Remsbottom 10.1 May L sample, various flows in the wakes, ch.p.w .: Gaseous fraction С, -С4 350 С atmospheric residue Mixture 350-520 ° С vacuum distillate 520 ° С vacuum residue IN 1IPI Order 4701/59 Circulation 464 Random polygons pr-tie, Uzhgorod, st. Project, 4 five 0 five 0 Mixture118,2 Deasphalted oil68,6 Asphalt bitumen 49,6 Part 8,2 The part that mattered the Cox test according to Remsbottom 38.6 May L product, C, the fraction of which has the meaning of coke test according to Remsbottom May 21.2 L41.4 Su - 350 ° С atmospheric distillate t 5.9 350 ° С vacuum distillate t30.9 350-520 ° С vacuum distillate 8.1 520 ° С vacuum residue22.8
权利要求:
Claims (1) [1] WITH; - 350 atmospheric distillate 39.1 350 ° C atmospheric residue42.6 Formula of the invention n and ; 35 oh whether 40 45 50 55 A method of producing distillate hydrocarbon fractions by processing heavy hydrocarbon feedstock containing asphaltenes, which includes the steps of thermal cracking, deasphalting, and catalytic hydroprocessing, characterized in that, in order to increase the yield of the target products, from thermal cracking products containing 3.3 8.4 wt.% Of the fraction C, -C, the distillate fractions and the cracking residue are separated, which is supplied either at the deasphalting stage, followed by feeding of the deasphalted product to the thermal cracking stage and lennoy asfaltobitumnoy fraction in step the catalytic hydrotreatment or for the catalytic hydrotreatment stage with separation of the products obtained in distillate fractions and a residual fraction which is fed to the deasphalting step of supplying a deasphalted product in the thermal cracking step. Subscription
类似技术:
公开号 | 公开日 | 专利标题 SU1424740A3|1988-09-15|Method of producing hydrocarbon distillate fractions US3287254A|1966-11-22|Residual oil conversion process US5462650A|1995-10-31|Process for producing low viscosity lubricating base oil having high viscosity index US4354928A|1982-10-19|Supercritical selective extraction of hydrocarbons from asphaltic petroleum oils CA1207270A|1986-07-08|Process for removing polymer-forming impurities fromnaphtha fraction US5024750A|1991-06-18|Process for converting heavy hydrocarbon oil US4126538A|1978-11-21|Process for the conversion of hydrocarbons JP2020533453A|2020-11-19|Low quality oil reforming method and reforming system US4405441A|1983-09-20|Process for the preparation of hydrocarbon oil distillates EP0082555B1|1985-11-21|Process for the production of hydrocarbon oil distillates US3132088A|1964-05-05|Visbreaking, deasphalting and hydrogenation of crude oils US3321395A|1967-05-23|Hydroprocessing of metal-containing asphaltic hydrocarbons RU2024586C1|1994-12-15|Process for treating heavy asphalthene-containing stock KR100188422B1|1999-06-01|Method of upgrading residua CA1243979A|1988-11-01|Process for increasing deasphalted oil productionfrom upgraded oil residua US5098551A|1992-03-24|Process for the manufacture of lubricating base oils CA1198387A|1985-12-24|Process for the production of low-asphalteneshydrocarbon mixtures WO2009014303A1|2009-01-29|Method for producing feedstocks of high quality lube base oil from coking gas oil US4721557A|1988-01-26|Combination process for the conversion of a residual asphaltene-containing hydrocarbonaceous stream to maximize middle distillate production EP0125709B1|1989-08-02|A process for the production of low-asphaltenes hydrocarbon mixtures EP0082551B1|1986-02-19|Process for the production of hydrocarbon oil distillates US3407134A|1968-10-22|Process for hydrocracking an asphaltic hydrocarbon feed stock in the presence of a hydrogenated hydrocarbon and hydrocaracking catalyst EP0090441B1|1985-10-09|Process for the production of deasphalted oil and hydrocarbon oil distillates EP0321713B1|1993-03-10|Production of high density jet fuel from coal liquids CA1196305A|1985-11-05|Petroleum residues by means of reduction of viscosity,deasphaltation and hydrotreatment
同族专利:
公开号 | 公开日 EP0090437A1|1983-10-05| CA1195638A|1985-10-22| ES520644A0|1983-12-16| JPS58201889A|1983-11-24| US4400264A|1983-08-23| MX162350A|1991-04-26| EP0090437B1|1985-12-04| NL8201119A|1983-10-17| AU1250583A|1983-09-22| AU555121B2|1986-09-11| DE3361368D1|1986-01-16| ZA831834B|1983-11-30| ES8401515A1|1983-12-16|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3281350A|1963-05-06|1966-10-25|Exxon Research Engineering Co|Hf deasphalting for hydrocracking feed preparation| US3781197A|1972-01-10|1973-12-25|Gulf Research Development Co|Process for cracking hydrocarbons containing hydrodesulfurized residual oil| US3775292A|1972-08-01|1973-11-27|Universal Oil Prod Co|Combination process for the conversion of hydrocarbonaceous black oil| US3775293A|1972-08-09|1973-11-27|Universal Oil Prod Co|Desulfurization of asphaltene-containing hydrocarbonaceous black oils| US3806444A|1972-12-29|1974-04-23|Texaco Inc|Desulfurization of petroleum crude| JPS5422444B2|1974-11-07|1979-08-07| JPS5422445B2|1975-01-31|1979-08-07| NL7507484A|1975-06-23|1976-12-27|Shell Int Research|PROCESS FOR CONVERTING HYDROCARBONS.| NL7510465A|1975-09-05|1977-03-08|Shell Int Research|PROCESS FOR CONVERTING HYDROCARBONS.| NL7610510A|1976-09-22|1978-03-28|Shell Int Research|METHOD FOR CONVERTING HYDROCARBONS.| NL7610511A|1976-09-22|1978-03-28|Shell Int Research|METHOD FOR CONVERTING HYDROCARBONS.| NL190815C|1978-07-07|1994-09-01|Shell Int Research|Process for the preparation of gas oil.| NL190816C|1978-07-07|1994-09-01|Shell Int Research|Process for the preparation of gas oil.| GB2031011B|1978-10-05|1983-01-06|Chiyoda Chem Eng Construct Co|Processing heavy hydrocarbon oils| JPS623198B2|1981-01-25|1987-01-23|Chiyoda Chem Eng Construct Co|NL8105660A|1981-12-16|1983-07-18|Shell Int Research|PROCESS FOR PREPARING HYDROCARBON OIL DISTILLATES| NL8201243A|1982-03-25|1983-10-17|Shell Int Research|PROCESS FOR THE PREPARATION OF LOW ASPHALTANE HYDROCARBON MIXTURE.| US4462895A|1983-02-25|1984-07-31|Exxon Research & Engineering Co.|Combination visbreaking and hydrorefining with recycle of hydrorefined bottoms| US4469587A|1983-09-02|1984-09-04|Intevep, S.A.|Process for the conversion of asphaltenes and resins in the presence of steam, ammonia and hydrogen| JPS6072989A|1983-09-30|1985-04-25|Res Assoc Residual Oil Process<Rarop>|Method for thermally cracking heavy oil| US4579646A|1984-07-13|1986-04-01|Atlantic Richfield Co.|Bottoms visbreaking hydroconversion process| CA1222471A|1985-06-28|1987-06-02|H. John Woods|Process for improving the yield of distillables inhydrogen donor diluent cracking| US4695367A|1986-03-24|1987-09-22|The M. W. Kellogg Company|Diesel fuel production| US4721557A|1986-10-08|1988-01-26|Uop Inc.|Combination process for the conversion of a residual asphaltene-containing hydrocarbonaceous stream to maximize middle distillate production| US5601697A|1994-08-04|1997-02-11|Ashland Inc.|Demetallation-High carbon conversion process, apparatus and asphalt products| ZA989153B|1997-10-15|1999-05-10|Equistar Chem Lp|Method of producing olefins and feedstocks for use in olefin production from petroleum residua which have low pentane insolubles and high hydrogen content| CA2281058C|1998-09-03|2008-08-05|Ormat Industries Ltd.|Process and apparatus for upgrading hydrocarbon feeds containing sulfur, metals, and asphaltenes| US6274003B1|1998-09-03|2001-08-14|Ormat Industries Ltd.|Apparatus for upgrading hydrocarbon feeds containing sulfur, metals, and asphaltenes| JP5057315B2|1998-10-30|2012-10-24|日揮株式会社|Method for producing gas turbine fuel oil| US7407571B2|2001-12-26|2008-08-05|Ormat Industries Ltd.|Method of and apparatus for upgrading and gasifying heavy hydrocarbon feeds| AT331014T|2002-12-20|2006-07-15|Eni Spa|CRACKING PROCESSES FOR HEAVY DUTIES SUCH AS HEAVY RAW OILS AND DISTILLATION SOLIDS| JP4498929B2|2002-12-30|2010-07-07|エニ、ソシエタ、ペル、アチオニ|Methods for converting heavy charges such as heavy crude oil and distillation residues| JP2006070230A|2004-09-06|2006-03-16|Nippon Oil Corp|Desulfurization method of heavy oil| FR2943069A1|2009-03-13|2010-09-17|Total Raffinage Marketing|Oil loads such as heavy hydrocarbon loads e.g. heavy crude oils, converting method, involves mixing loads at cut distilating from five hundred degree Celsius to size hundred degree Celsius before conversion treatment| CA2963436A1|2017-04-06|2018-10-06|Iftikhar Huq|Partial upgrading of bitumen|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 NL8201119A|NL8201119A|1982-03-18|1982-03-18|PROCESS FOR PREPARING HYDROCARBON OIL DISTILLATES| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|